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About This Item
Linear Formula:
CH3COOAg
CAS Number:
Molecular Weight:
166.91
UNSPSC Code:
12352103
NACRES:
NA.21
PubChem Substance ID:
EC Number:
209-254-9
Beilstein/REAXYS Number:
3595636
MDL number:
Assay:
99%
Form:
powder or chunks
Product Name
Silver acetate, ReagentPlus®, 99%
InChI key
CQLFBEKRDQMJLZ-UHFFFAOYSA-M
InChI
1S/C2H4O2.Ag/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1
SMILES string
CC(O[Ag])=O
product line
ReagentPlus®
assay
99%
form
powder or chunks
reaction suitability
reagent type: catalyst
core: silver
Quality Level
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Application
Used in a novel preparation of highly reflective, conductive silvered polymer films. Also effectively catalyzes cycloaddition reactions of isocyanoacetates with a variety of olefins.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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cis-Hydroxylation of a synthetic steroid intermediate with iodine, silver acetate and wet acetic acid.
Woodward RB and Brutcher Jr FV.
Journal of the American Chemical Society, 80(1), 209-211 (1958)
Silver acetate catalysed cycloadditions of isocyanoacetates.
Grigg R, et al.
Tetrahedron, 55(7), 2025-2044 (1999)
Study of thermal decomposition of silver acetate.
Logvinenko V, et al.
Journal of Thermal Analysis and Calorimetry, 90(3), 813-816 (2007)
Grigg, R. et al.
Tetrahedron, 55, 2025-2025 (1999)
Silver acetate-assisted formation of amides from acyl chlorides.
Leggio A, et al.
Tetrahedron Letters, 56(1), 199-202 (2015)
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